Canonical Allele Identifier: CA419932418

Gene: VTCN1

Linked Data

• gnomAD v4: 1-117147739-T-G
• MyVariant Identifiers: chr1:g.117690361T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147739T>G , CM000663.2:g.117147739T>G	GRCh38
NC_000001.10:g.117690361T>G , CM000663.1:g.117690361T>G	GRCh37
NC_000001.9:g.117491884T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.768A>C MANE Select	ENSP00000358470.3:p.Ser256=
ENST00000328189.7:c.420A>C	ENSP00000328168.3:p.Ser140=
ENST00000359008.8:c.777A>C	ENSP00000351899.4:p.Ser259=
ENST00000369458.7:c.768A>C	ENSP00000358470.3:p.Ser256=
ENST00000539893.5:c.483A>C	ENSP00000444724.1:p.Ser161=
NM_001253849.1:c.483A>C	NP_001240778.1:p.Ser161=
NM_001253850.1:c.420A>C	NP_001240779.1:p.Ser140=
NM_024626.3:c.768A>C	NP_078902.2:p.Ser256=
NR_045603.1:n.963A>C
NR_045604.1:n.667A>C
XM_011542143.1:c.819A>C	XP_011540445.1:p.Ser273=
XM_011542144.1:c.822A>C	XP_011540446.1:p.Ser274=
XM_011542145.1:c.783A>C	XP_011540447.1:p.Ser261=
XM_011542143.2:c.918A>C	XP_011540445.2:p.Ser306=
XM_017002335.2:c.783A>C	XP_016857824.1:p.Ser261=
NM_024626.4:c.768A>C MANE Select	NP_078902.2:p.Ser256=
NR_045603.2:n.930A>C
NR_045604.2:n.634A>C
NM_001253849.2:c.483A>C	NP_001240778.1:p.Ser161=
NM_001253850.2:c.420A>C	NP_001240779.1:p.Ser140=